HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587801Generated: October 30, 2026
CID 71433830 → N-((1R,2S)-1-benzyl-7-bromo-1,2,3,4-tetrahydronaphthalen-2-yl)propionamide
https://huagongshe.com/reaction/587801
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | CID 71433830 | HCID 71433830 | — |
| Reactant | N-(1-benzyl-7-bromo-3,4-dihydronaphthalen-2-yl)propionamide | HCID 86707883 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178478078 | HCID 178478078 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-((1R,2S)-1-benzyl-7-bromo-1,2,3,4-tetrahydronaphthalen-2-yl)propionamide | HCID 72707166 | 68% |
Reaction Steps
Chlorocyclooctadiene rhodium(I) dimer (0.217 g, 0.881 mmol of Rh), Josiphos SL-J216-2 (0.595 g, 0.926 mmol), and N-(1-benzyl-7-bromo-3,4-dihydronaphthalen-2-yl)propionamide (10.88 g, 29.4 mmol) were combined in a metal reactor, and the vessel was inerted with argon. Degassed ethanol (163 ml) was added, and the mixture was agitated under argon for 30 min at 50° C. The vessel was pressurized with 60 psig of hydrogen and agitated at 55° C. for 14.5 hrs. HPLC analysis indicated 89.4% conversion and 93.8% ee. The mixture was concentrated, and the resulting solid was crystallized from MeOH to yield 7.41 g (yield: 68%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227901B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-48e0a33ec1524d12ba330d599da8f15b |
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| Source note | uspto-grants-2016_01 |
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